Search Results - "CHANDAK, G.R."

Pancreatitis associated chymotrypsin C (CTRC) mutations show distinct loss-of-function phenotypes by Beer, S, Zhou, J, Szabó, A, Keiles, S, Chandak, G.R, Witt, H, Sahin-Tóth, M

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Apolipoprotein E and Presenilin-1 Allelic Variation and Alzheimer's Disease in India by CHANDAK, G.R., SRIDEVI, M. UMA, VAS, C.J., PANIKKER, D.M., SINGH, L.

“…As part of a larger epidemiological survey to study the prevalence of dementia in a suburb of Mumbai, Western India, we identified 78 cases with a Clinical…”
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Novel p.P298L SURF1 mutation in thiamine deficient Leigh syndrome patients compromises cytochrome c oxidase activity by Mani, Shalini, Chandak, G.R., Singh, Keshav K., Singh, Rajender, Rao, S. Narasimha

“…•Different novel and reported nucleotide variations were reported in thiamine responsive Leigh syndrome patients.•Following different in-silico tests, 2…”
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Some Atypical and Rare Sickle Cell Gene Haplotypes in Populations of Andhra Pradesh, India by NIRANJAN, Y., CHANDAK, G.R., VEERRAJU, P., SINGH, LALJI

“…We have investigated the clinical, hematological, and molecular genetic characteristics of sickle cell anemia patients from 6 populations of Andhra Pradesh,…”
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Sickle Cell Gene Haplotypes in Relli and Thurpu Kapu Populations of Andhra Pradesh by RAMANA, G.V., CHANDAK, G.R., SINGH, L.

“…We performed polymerase chain reaction analysis of 8 restriction-site polymorphisms in the β-globin gene cluster to define haplotypes and provide hematological…”
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Association of common variants in/near six genes (ATP2B1, CSK, MTHFR, CYP17A1, STK39 and FGF5) with blood pressure/hypertension risk in Chinese children by Xi, B, Shen, Y, Zhao, X, Chandak, G R, Cheng, H, Hou, D, Li, Y, Ott, J, Zhang, Y, Wang, X, Mi, J

“…Recent genome-wide association studies have identified several single-nucleotide polymorphisms (SNPs) that are associated with blood pressure…”
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Lack of replication of association of THSD7A with obesity by Ahmad, M, Nongmaithem, S S, Krishnaveni, G V, Fall, C H D, Yajnik, C S, Chandak, G R

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Mutations in the pancreatic secretory trypsin inhibitor gene by Chandak, G.R, Idris, M.M, Reddy, D.N, Bhaskar, S, Sriram, P.V.J, Singh, L

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Juvenile fibrocalculous pancreatopathy--a patient report by Bashir, Mir Iftikhar, Misgar, Raiz Ahmad, Wani, Arshad Iqbal, Gupta, Vipen, Masoodi, Shariq Rashid, Chandak, Giriraj Ratan, Zargar, Abdul Hamid

“…Fibrocalculous pancreatopathy (FCPP) is a secondary form of diabetes mellitus (DM) with obscure etiology. Recently various gene mutations have been reported in…”
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Fetus-in-fetu: A case report with molecular analysis by Kumar, A.Narendra, Chandak, G.R., Rajasekhar, A., Reddy, N.C.K., Singh, L.

“…This is the report of a case of fetus-in-fetu diagnosed in a 3-month-old boy and found to be located in the upper retroperitoneum. The entity was distinguished…”
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